Career as Clinical Research Associate in ICON

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ICON is a global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. We specialize in the strategic development, management and analysis of programs that support Clinical Development – from compound selection to Phase I - IV clinical studies
ICON enjoys a strong reputation for quality and is focused on staff development. We make it our mission to attract the most diverse and creative minds into the business and we continually strive to provide opportunities for our people to excel, grow and build a great career. We understand that our greatest asset is the skills and talents of our people and they are truly what set us apart.

Post: Clinical Research Associate

Job Description
Working within a highly qualified team you will identify, select, initiate and close-out investigational sites for clinical studies in phases II – III ensuring that applicable regulations and principles of ICG-GCP are adhered to
- Working independently and proactively to coordinate all necessary activities required to set up and monitor a study, completing accurate study status reports and maintaining study documentation
- Submission of protocol, consent documents for ethics/IRB approval and assist in preparing regulatory submissions as requested
- Participate in preparing and reviewing study documentation and feasibility studies for new proposals as required
- Managing sponsor generated queries efficiently and responsible for study cost effectiveness
- Dependent on level of experience you may assist in training and mentoring less experienced CRA’s and/or manage CRA’s working on international projects

Experience and Qualification
- 1+ years of monitoring experience in phase I~III trials as a CRA
- Knowledge of ICG GCP guidelines and expertise to review and evaluate medical data
- Fluent in English as well as the local language
- Excellent communication and interpersonal skills, both written and verbal enabling you to deal with queries in a timely manner
- Ability to produce accurate work to tight deadlines within a pressurized environment
- Computer literate with Microsoft Office
- Must be available to travel international and domestic at least 60% fly
- Must hold a bachelor’s degree in pharmacy, nursing, science, or equivalent

Additional Information:
Qualification:
Bachelor’s degree
Location
:
Bangalore
Reference: 015900
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: CR
End Date:
5th September, 2015

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